US2267548A - Art of extracting oil from the - Google Patents
Art of extracting oil from the Download PDFInfo
- Publication number
- US2267548A US2267548A US2267548DA US2267548A US 2267548 A US2267548 A US 2267548A US 2267548D A US2267548D A US 2267548DA US 2267548 A US2267548 A US 2267548A
- Authority
- US
- United States
- Prior art keywords
- oil
- earth
- water
- acid
- mother
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000003921 oil Substances 0.000 description 37
- 239000011435 rock Substances 0.000 description 21
- 239000007864 aqueous solution Substances 0.000 description 14
- 239000002253 acid Substances 0.000 description 13
- 239000000243 solution Substances 0.000 description 12
- 239000000126 substance Substances 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000003795 chemical substances by application Substances 0.000 description 10
- -1 oleates Chemical class 0.000 description 9
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 239000011269 tar Substances 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 4
- 239000003129 oil well Substances 0.000 description 4
- 238000009736 wetting Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 235000019738 Limestone Nutrition 0.000 description 3
- 239000010779 crude oil Substances 0.000 description 3
- 159000000011 group IA salts Chemical class 0.000 description 3
- 239000006028 limestone Substances 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 159000000007 calcium salts Chemical class 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000010459 dolomite Substances 0.000 description 2
- 229910000514 dolomite Inorganic materials 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 description 2
- 229960000907 methylthioninium chloride Drugs 0.000 description 2
- 238000005086 pumping Methods 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- XZSUEVFAMOKROK-UHFFFAOYSA-N 1,2-dihydroxy-3-nitroanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(O)=C(O)C([N+]([O-])=O)=C2 XZSUEVFAMOKROK-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- ATJXMQHAMYVHRX-CPCISQLKSA-N Ellagic acid Natural products OC1=C(O)[C@H]2OC(=O)c3cc(O)c(O)c4OC(=O)C(=C1)[C@H]2c34 ATJXMQHAMYVHRX-CPCISQLKSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- JTXJZBMXQMTSQN-UHFFFAOYSA-N amino hydrogen carbonate Chemical class NOC(O)=O JTXJZBMXQMTSQN-UHFFFAOYSA-N 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical class OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- ZXJXZNDDNMQXFV-UHFFFAOYSA-M crystal violet Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1[C+](C=1C=CC(=CC=1)N(C)C)C1=CC=C(N(C)C)C=C1 ZXJXZNDDNMQXFV-UHFFFAOYSA-M 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000001495 ethyl group Chemical class [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 239000008396 flotation agent Substances 0.000 description 1
- 235000021588 free fatty acids Nutrition 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000003077 lignite Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical class [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 150000002942 palmitic acid derivatives Chemical class 0.000 description 1
- 238000005504 petroleum refining Methods 0.000 description 1
- 150000004707 phenolate Chemical class 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- ZHFPEICFUVWJIS-UHFFFAOYSA-M sodium 2-hydroxy-5-[(3-nitrophenyl)diazenyl]benzoate Chemical compound [Na+].Oc1ccc(cc1C([O-])=O)N=Nc1cccc(c1)[N+]([O-])=O ZHFPEICFUVWJIS-UHFFFAOYSA-M 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical class [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 150000003566 thiocarboxylic acids Chemical class 0.000 description 1
- 239000011276 wood tar Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/58—Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids
- C09K8/584—Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids characterised by the use of specific surfactants
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S507/00—Earth boring, well treating, and oil field chemistry
- Y10S507/933—Acidizing or formation destroying
Definitions
- the present invention relates to the art of extracting oil from the earth.
- a further object of the present invention is to pump aqueous solutions containing wetting agents possessing some solubility in oil into the earth adjacent to the well to release from the mother rock residual oil locked therein.
- the invention likewise contemplates the provision of a process of utilizing capillary active sub.-. stances to eifect the removal of imprisoned oil and of utilizing aqueous solutions of the aforesaid substances containing the so-called "polar" groups.
- the invention comprises releasing the oil and freeing it from the surrounding rocks to enable the oil to flow together in a mass or pool from which it may be removed to the surface of the earth. It has been found that capillarity phenomena cause the adhesion of oil utilizing a watery solution containing an organic oil soluble and water soluble wetting agent and by pumping this solution into a region containing imprisoned oil, the walls of the rock and even the capillary spaces are moistened and wetted by the wetting solutions and the bond between the oil and the mother rock is disrupted. It is believed that the wetting substance forms a film over the surface of the rock which enables the oil to form droplets and globules and to collect together in a mass. In this manner, the oil is freed from the mother rock, even the capillary spaces, and the oil can then be easily separated from the rock and removed from the interior of the earth.
- aqueous solutions containing wetting substances are effective to release the imprisoned oil from the mother rock and to enable the thusreleased oil to run together and to be collected to the surfaces of the walls of mother rock.
- soaps -known as soaps.
- oil-liberating agents are phenols or aromatic amino compounds, etc., such as aniline and its homologues, amido phenols, phenol-sulfonic acids, amido sulfonic acids, alcohols with long carbon chains, alcohol sulfonates, xanthogenates and/or combinations thereof.
- Aqueous solutions of suitable organic dyestuifs may be advantageously used as oil-liberating agents.
- hasic dyestuffs such as crystal violet and methylene blue, or acid dyestuffs (in weak acid solutions. if necessary), such as "cloth red and alizarin yellow.
- a diluted solution say about (Ll-%, of an alkaline salt, such, for instance, a sodium salt of the so-called tar acids may be used as the oilliberating agent for removal of crude oil adhering to "hydrophile rocks, such as sandstone, limestone, dolomite, etc.
- the so-called water-soluble tar acids may be made, for instance, according to U. S. Patent No. 1,812,316 or made by adding to water-soluble tar acids of the acid wash in petroleum refining, the alkaline wash liquids from the purification of crude oil fractions.
- water solutions of free tar acids or/and their acid salts may also be used, especially in the case of acid rock like sandstone.
- Aqueous solutions of mineral coal, brown coal or wood tar phenols or phenolates have been used as oil-liberating agents as in Example No. 1 with satisfactory results. With these agents, it has been noticed that a quick, practical and substantially complete liberation of the oil is effected in the mother rock and that the removal of the liberated oil may be effected.
- Aqueous solutions of aniline at ordinary or increased temperature have been used to great advantage for the liberation and removal of oil.
- Aqueous solution of alkaline salts of ethyl or amyl xanthogenates or alkaline salts of higher alcohol sulfonates or of benzol sulfonic acids or their homologues or amino phenols or aromatic amino sulfonic acids or/and the corresponding free compounds may. be used for the purpose of liberating and removing oil.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
?atented Dec. 23, 1941 HE S ART OF EXTRACTJING OIL FROM THE EARTH Ernst Berl, Pittsburgh, Pa.
No Drawing. Application January 31, 1936, Se-
rial No. 61,804. In Great Britain February 4,
4 Claims.
The present invention relates to the art of extracting oil from the earth.
It has been well known that, heretofore, the extraction of oil from the earth has been very incomplete. Tests have demonstrated that considerable quantities of crude oil remained in the mother rock, such as limestone, sandstone, and the like. In some instances, it has been found that about 20% to about 70% of oil remained in the rocks in the earth. The residual oil left in the earth has been considered lost for all practical purposes. Various proposals have been made to avoid the losses which have been experienced in the past. Of these proposals, men tion may be made of the attempts to pump or force water down wells surrounding the oil well which has been undergoing pumping. In some cases, salt or soda has been added to the water. In a few isolated cases, some results were obtained, but in most cases the results have been unfavorable. None of the attempts, as far as I am aware, has been wholly satisfactory, particularly when carried into practice on an industrial scale.
I have discovered that the aforesaid losses of oil remaining in the mother rock can be reduced and that considerable improvements in the yields can be effected from oil wells.
It is an object of the present invention to overcome the unfavorable conditions in the exploitation and recovery of oil from the earth and to utilize an aqueous solution containing substances possessing stronger wetting properties than water for removing oil from the mother rock.
A further object of the present invention is to pump aqueous solutions containing wetting agents possessing some solubility in oil into the earth adjacent to the well to release from the mother rock residual oil locked therein.
The invention likewise contemplates the provision of a process of utilizing capillary active sub.-. stances to eifect the removal of imprisoned oil and of utilizing aqueous solutions of the aforesaid substances containing the so-called "polar" groups.
Other advantages and objects of the invention will become apparent from the following description.
Broadly stated, the invention comprises releasing the oil and freeing it from the surrounding rocks to enable the oil to flow together in a mass or pool from which it may be removed to the surface of the earth. It has been found that capillarity phenomena cause the adhesion of oil utilizing a watery solution containing an organic oil soluble and water soluble wetting agent and by pumping this solution into a region containing imprisoned oil, the walls of the rock and even the capillary spaces are moistened and wetted by the wetting solutions and the bond between the oil and the mother rock is disrupted. It is believed that the wetting substance forms a film over the surface of the rock which enables the oil to form droplets and globules and to collect together in a mass. In this manner, the oil is freed from the mother rock, even the capillary spaces, and the oil can then be easily separated from the rock and removed from the interior of the earth.
In carrying the present invention into practice, I have found that aqueous solutions containing wetting substances, especially capillary-active substances, are effective to release the imprisoned oil from the mother rock and to enable the thusreleased oil to run together and to be collected to the surfaces of the walls of mother rock. By
- known as soaps.
and removed from its native environment. As a result of extensive experiments, I have discovered that aqueous solutions containing socalled water-soluble tar acids and/or salts thereof have given satisfactory results. In addition, substances having similar constitution containing so-called polar groups, such as OH, NH2, COOH, SOaH, CSSH and their combinations associated with straight chain hydrocarbons, aromatic ring compounds, etc. etc. are within the purview of the present invention. Thus, satisfactory results have been given by free fatty acids, such as oleic acid, palmitic acid, stearic acid, etc. which contain long carbon chains and/or their salts, such as oleates, palmitates, stearates, etc. which are Other examples of oil-liberating agents are phenols or aromatic amino compounds, etc., such as aniline and its homologues, amido phenols, phenol-sulfonic acids, amido sulfonic acids, alcohols with long carbon chains, alcohol sulfonates, xanthogenates and/or combinations thereof. Aqueous solutions of suitable organic dyestuifs may be advantageously used as oil-liberating agents. For instance, hasic dyestuffs, such as crystal violet and methylene blue, or acid dyestuffs (in weak acid solutions. if necessary), such as "cloth red and alizarin yellow. As further examples of oil-liberating agents, mention may be made of substances used in flotation. A fairly complete list of these flotation agents may be found in Taggarts Handbook of Ore Dressing (1927 edition, pages 830 to 839).
For the purpose of giving those skilled in the art a better understanding of the invention, the following illustrative examples are given.
Example N0. 1
A diluted solution, say about (Ll-%, of an alkaline salt, such, for instance, a sodium salt of the so-called tar acids may be used as the oilliberating agent for removal of crude oil adhering to "hydrophile rocks, such as sandstone, limestone, dolomite, etc. The so-called water-soluble tar acids may be made, for instance, according to U. S. Patent No. 1,812,316 or made by adding to water-soluble tar acids of the acid wash in petroleum refining, the alkaline wash liquids from the purification of crude oil fractions. For the same purpose, water solutions of free tar acids or/and their acid salts, may also be used, especially in the case of acid rock like sandstone. In this manner, a substantially complete removal of the oil, even in the fine capillaries, may be eifected' In contrast to the foregoing, if water is used in accordance with prior art teachings in place of the aqueous solutions mentioned herein, it has been observed that an emulsion of the oil with water formed and that an incomplete removal of the oil occurs.
In applying my solutions of oil-liberating agents, it is preferred to pump an aqueous solution containing the same into the earth surrounding the oil well through one or more pipes. For
' instance, it is preferred to use four pipes surrounding the oil well, preferably in the form of a quadrangle.
Example No. 2
Aqueous solutions of mineral coal, brown coal or wood tar phenols or phenolates have been used as oil-liberating agents as in Example No. 1 with satisfactory results. With these agents, it has been noticed that a quick, practical and substantially complete liberation of the oil is effected in the mother rock and that the removal of the liberated oil may be effected.
Example No. 3
Aqueous solutions of aniline at ordinary or increased temperature have been used to great advantage for the liberation and removal of oil.
Example No. 4
Aqueous solution of alkaline salts of ethyl or amyl xanthogenates or alkaline salts of higher alcohol sulfonates or of benzol sulfonic acids or their homologues or amino phenols or aromatic amino sulfonic acids or/and the corresponding free compounds may. be used for the purpose of liberating and removing oil. One may also use for the same purpose aqueous solutions of amido phenols and amino phenolates, amido carbonic acids or/and their salts and mixtures of the substances mentioned in this example or in the foregoing examples. Excellent results have been obtained by their use.
Example No. 5
A diluted aqueous solution of methyl violet or methylene blue has been found to give satisfactory results for the liberation and removal of oil.
Example No. 6
Satisfactory results have been obtained by the use of solutions of acid organic dyestufis, such as cloth" red or alizarin orange.
Although the present invention has been de scribed in conjunction with certain preferred embodiments it is to be understood that variations and modifications may be resorted to without departing from the spirit and scope of the invention as described herein and defined in the appended claims. Thus, substances which contain the socalled carbophile and hydrpphile groups or constituents may be used. In addition to those mentioned hereinbefore, substances containing the following groups may be included: =NH, =8, -SH, CSN, and CSNH. For best results, sodium salts of water-soluble acid tars and alcohol sulionates are preferred. Certain advantages may be obtained in using such substances which will give soluble calcium salts because the greatest part of mother rocks which contain oil are formed of limestone or dolomite. When aqueous solutions of a substance which produces an insoluble calcium salt are used, capillaries and fine fissures tend to become clogged and certain difiiculties toward the liberation and free flow of oil are encountered.
I claim:
1. The process of extracting oil from the earth in regions adjacent to mother rocks, which comprises introducing into such regions a water solution having no substantial destructive effect upon said mother rocks and comprising an organic oil soluble and water soluble substance containing a polar group and free from sulfonic acid groups in the molecule.
2. The process of extracting oil from the earth in regions adjacent to mother rocks which comprises introducing into said regions an oil-freeing agent comprising a water solution of an aromatic compound of the group consisting of aniline, amino phenols, amino phenolates, phenols, and amino carbonic acids.
3. The process of extracting oil from the earth in regions adjacent to mother rocks which comprises introducing into said regions an oil-freeing agent comprising a water solution of an aromatic dyestuf! of the group consisting of basic and acid of benzene, naphthalene, anthracene and thioanthracene compounds.
4. The process of extracting oil rrbm the earth in regions adjacent to mother rockswhich comprises introducing into said regions an oil-freeing agent comprising a water solution of a salt of a thiocarboxylic acid having not more than six carbon atoms.
ERNST BERL.
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2267548A true US2267548A (en) | 1941-12-23 |
Family
ID=3432351
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US2267548D Expired - Lifetime US2267548A (en) | Art of extracting oil from the |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2267548A (en) |
Cited By (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2419755A (en) * | 1943-05-26 | 1947-04-29 | Union Oil Co | Chemical treatment of oil sands |
| US2465237A (en) * | 1937-03-31 | 1949-03-22 | Delmar H Larsen | Treatment of oil wells |
| US2765851A (en) * | 1953-09-23 | 1956-10-09 | Pure Oil Co | Process for improving oil recovery processes |
| US2833711A (en) * | 1954-10-04 | 1958-05-06 | Sinclair Oil & Gas Company | Method of treating brine disposal wells and composition therefor |
| US3079336A (en) * | 1960-03-22 | 1963-02-26 | Jersey Prod Res Co | Alcohols in conjunction with water thickeners for a secondary recovery process |
| US3131759A (en) * | 1959-06-19 | 1964-05-05 | Socony Mobil Oil Co Inc | Method of treating oil-productive subterranean formations |
| US3137345A (en) * | 1960-07-29 | 1964-06-16 | Phillips Petroleum Co | Increasing miscible flooding efficiencies |
| US3167119A (en) * | 1961-04-04 | 1965-01-26 | Jersey Prod Res Co | Oil reservoir depletion process |
| US3391736A (en) * | 1964-03-16 | 1968-07-09 | Mobil Oil Corp | Liquid flow in a permeable earth formation |
| US3593790A (en) * | 1969-01-02 | 1971-07-20 | Shell Oil Co | Method for producing shale oil from an oil shale formation |
| US3601197A (en) * | 1970-04-29 | 1971-08-24 | Exxon Production Research Co | Treatment of formations with aryl sulfonic acid |
| US3612178A (en) * | 1969-10-20 | 1971-10-12 | Walter F Germer Jr | Method of recovering oil using flow stimulating solution |
| US3796266A (en) * | 1972-12-13 | 1974-03-12 | Texaco Inc | Surfactant oil recovery process |
| US3924685A (en) * | 1974-12-20 | 1975-12-09 | Texaco Inc | Method for oil recovery |
| US3926255A (en) * | 1974-11-07 | 1975-12-16 | Mobil Oil Corp | Waterflooding employing surfactants derived from metallic soaps |
| US3929190A (en) * | 1974-11-05 | 1975-12-30 | Mobil Oil Corp | Secondary oil recovery by waterflooding with extracted petroleum acids |
| US5053149A (en) * | 1990-03-30 | 1991-10-01 | Atochem North America, Inc. | Method for dewaxing oil and gas pipelines or wells |
| FR2735524A1 (en) * | 1995-06-13 | 1996-12-20 | Inst Francais Du Petrole | METHOD FOR ASSISTED RECOVERY OF PETROLEUM FLUIDS IN A SUBTERRANEAN FIELD |
| US10933381B1 (en) | 2011-04-26 | 2021-03-02 | Mansour S. Bader | Relative wettability: wet oil separation by a membrane |
-
0
- US US2267548D patent/US2267548A/en not_active Expired - Lifetime
Cited By (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2465237A (en) * | 1937-03-31 | 1949-03-22 | Delmar H Larsen | Treatment of oil wells |
| US2419755A (en) * | 1943-05-26 | 1947-04-29 | Union Oil Co | Chemical treatment of oil sands |
| US2765851A (en) * | 1953-09-23 | 1956-10-09 | Pure Oil Co | Process for improving oil recovery processes |
| US2833711A (en) * | 1954-10-04 | 1958-05-06 | Sinclair Oil & Gas Company | Method of treating brine disposal wells and composition therefor |
| US3131759A (en) * | 1959-06-19 | 1964-05-05 | Socony Mobil Oil Co Inc | Method of treating oil-productive subterranean formations |
| US3079336A (en) * | 1960-03-22 | 1963-02-26 | Jersey Prod Res Co | Alcohols in conjunction with water thickeners for a secondary recovery process |
| US3137345A (en) * | 1960-07-29 | 1964-06-16 | Phillips Petroleum Co | Increasing miscible flooding efficiencies |
| US3167119A (en) * | 1961-04-04 | 1965-01-26 | Jersey Prod Res Co | Oil reservoir depletion process |
| US3391736A (en) * | 1964-03-16 | 1968-07-09 | Mobil Oil Corp | Liquid flow in a permeable earth formation |
| US3593790A (en) * | 1969-01-02 | 1971-07-20 | Shell Oil Co | Method for producing shale oil from an oil shale formation |
| US3612178A (en) * | 1969-10-20 | 1971-10-12 | Walter F Germer Jr | Method of recovering oil using flow stimulating solution |
| US3601197A (en) * | 1970-04-29 | 1971-08-24 | Exxon Production Research Co | Treatment of formations with aryl sulfonic acid |
| US3796266A (en) * | 1972-12-13 | 1974-03-12 | Texaco Inc | Surfactant oil recovery process |
| US3929190A (en) * | 1974-11-05 | 1975-12-30 | Mobil Oil Corp | Secondary oil recovery by waterflooding with extracted petroleum acids |
| US3926255A (en) * | 1974-11-07 | 1975-12-16 | Mobil Oil Corp | Waterflooding employing surfactants derived from metallic soaps |
| US3924685A (en) * | 1974-12-20 | 1975-12-09 | Texaco Inc | Method for oil recovery |
| US5053149A (en) * | 1990-03-30 | 1991-10-01 | Atochem North America, Inc. | Method for dewaxing oil and gas pipelines or wells |
| FR2735524A1 (en) * | 1995-06-13 | 1996-12-20 | Inst Francais Du Petrole | METHOD FOR ASSISTED RECOVERY OF PETROLEUM FLUIDS IN A SUBTERRANEAN FIELD |
| US5758727A (en) * | 1995-06-13 | 1998-06-02 | Institut Francais Du Petrole | Enhanced petroleum fluid recovery method in an underground reservoir |
| US10933381B1 (en) | 2011-04-26 | 2021-03-02 | Mansour S. Bader | Relative wettability: wet oil separation by a membrane |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2267548A (en) | Art of extracting oil from the | |
| US3131759A (en) | Method of treating oil-productive subterranean formations | |
| US4270609A (en) | Tar sand extraction process | |
| US4194565A (en) | Surfactant oil recovery method for use in high temperature formations containing water having high salinity and hardness | |
| US3498379A (en) | Flooding method for recovering petroleum employing aqueous solution of hydrocarbon sulfonate | |
| US2419755A (en) | Chemical treatment of oil sands | |
| RU2633842C2 (en) | Composition of surfactant for recoverying underground liquid fossil fuel | |
| US3532168A (en) | Cementing process using micellar solutions as well pipe and formation face cleansers | |
| US4295980A (en) | Waterflood method | |
| US3480080A (en) | Waterflooding with an aqueous,saline solution of a hydrocarbon sulfonate having an optimum degree of sulfonation | |
| US3491834A (en) | Surfactant injection process | |
| USRE23360E (en) | Art of extracting oil from | |
| US3301328A (en) | Well stimulation | |
| US3554286A (en) | Recovery of hydrocarbons from subterranean hydrocarbon-bearing formations | |
| US2874779A (en) | Oil well treating method | |
| US2168315A (en) | Method for the purification of petroleum mahogany sulphonates | |
| US2403972A (en) | Process for extracting an aromatic hydrocarbon from a mixture containing other hydrocarbons | |
| ES8405878A1 (en) | Composition and method for cleaning hydrocarbon oil from hard surfaces. | |
| US2927639A (en) | Surfactant treatment of oil and gas wells | |
| US4732690A (en) | Oil recovery composition | |
| US2548630A (en) | Method of preventing corrosion in pipe-line transportation of refined petroleum oils | |
| US3283812A (en) | Surfactant for petroleum recovery | |
| Bartell et al. | Displacement of Crude Oil and Benzene from Silica by Aqueous Solutions | |
| US4504399A (en) | Surfactant and process for enhanced oil recovery | |
| US3076760A (en) | Composition for preventing acid sludge in oil well acidizing processes |